Oncology Clinical Researcher
Behavioral Health Market Context
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Job Description
lects real-world regulatory, scientific, and clinical standards.
Organization: Alignerr Position: Oncology Clinical Researcher Type: Hourly Contract Compensation: $40$80/hour Location: Remote Commitment: 1040 hours/week
What You'll Do:
• Design and run oncology clinical trials by developing study protocols, overseeing patient enrollment, and ensuring compliance with regulatory and ethical standards.
• Analyze cancer trial data, including safety, efficacy, and biomarker results, to evaluate how well treatments perform.
• Translate trial outcomes into regulatory and scientific reports used for FDA/EMA submissions, publications, and clinical decision-making.
• Review and evaluate AI-generated clinical insights for accuracy, clinical relevance, and regulatory alignment.
What We're Looking For:
• Experience designing and managing oncology clinical trials from protocol development through data readout.
• Strong background in analyzing oncology clinical data, including endpoints, safety profiles, and biomarkers.
• Familiarity with regulatory submission standards for agencies such as the FDA or EMA.
Preferred:
• Prior experience with data annotation, data quality, or evaluation systems
Why Join Us:
• Competitive pay and flexible remote work.
• Work directly on frontier AI systems transforming cancer research.
• Influence how AI models understand and reason about real oncology data.
• Freelance perks: autonomy, flexibility, and global collaboration.
• Potential for contract extension.
Application Process (Takes 1520 min)
• Submit your resume
• Complete a short screening
• Project matching and onboarding
PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
Organization: Alignerr Position: Oncology Clinical Researcher Type: Hourly Contract Compensation: $40$80/hour Location: Remote Commitment: 1040 hours/week
What You'll Do:
• Design and run oncology clinical trials by developing study protocols, overseeing patient enrollment, and ensuring compliance with regulatory and ethical standards.
• Analyze cancer trial data, including safety, efficacy, and biomarker results, to evaluate how well treatments perform.
• Translate trial outcomes into regulatory and scientific reports used for FDA/EMA submissions, publications, and clinical decision-making.
• Review and evaluate AI-generated clinical insights for accuracy, clinical relevance, and regulatory alignment.
What We're Looking For:
• Experience designing and managing oncology clinical trials from protocol development through data readout.
• Strong background in analyzing oncology clinical data, including endpoints, safety profiles, and biomarkers.
• Familiarity with regulatory submission standards for agencies such as the FDA or EMA.
Preferred:
• Prior experience with data annotation, data quality, or evaluation systems
Why Join Us:
• Competitive pay and flexible remote work.
• Work directly on frontier AI systems transforming cancer research.
• Influence how AI models understand and reason about real oncology data.
• Freelance perks: autonomy, flexibility, and global collaboration.
• Potential for contract extension.
Application Process (Takes 1520 min)
• Submit your resume
• Complete a short screening
• Project matching and onboarding
PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
Qualifications
- •Experience designing and managing oncology clinical trials from protocol development through data readout
- •Strong background in analyzing oncology clinical data, including endpoints, safety profiles, and biomarkers
- •Familiarity with regulatory submission standards for agencies such as the FDA or EMA
- •Project matching and onboarding
Benefits
- •Organization: Alignerr Position: Oncology Clinical Researcher Type: Hourly Contract Compensation: $40$80/hour Location: Remote Commitment: 1040 hours/week
- •Competitive pay and flexible remote work
- •Work directly on frontier AI systems transforming cancer research
- •Influence how AI models understand and reason about real oncology data
- •Freelance perks: autonomy, flexibility, and global collaboration
- •Potential for contract extension
Responsibilities
- •In this role, you will ensure that oncology trial data used to train and assess advanced AI systems reflects real-world regulatory, scientific, and clinical standards
- •Design and run oncology clinical trials by developing study protocols, overseeing patient enrollment, and ensuring compliance with regulatory and ethical standards
- •Analyze cancer trial data, including safety, efficacy, and biomarker results, to evaluate how well treatments perform
- •Translate trial outcomes into regulatory and scientific reports used for FDA/EMA submissions, publications, and clinical decision-making
- •Review and evaluate AI-generated clinical insights for accuracy, clinical relevance, and regulatory alignment
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